Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children-Reference-Cited by-同舟云学术

Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children

Published:2021-09-20 Issue:20 Volume:25 Page:9609-9616
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cell Mol Med

Author:

Lan Chaoting¹,Wu Yuxin¹,Wang Ning²^ORCID,Luo Yun³,Zhao Jinglu⁴,Zheng Yi⁴^ORCID,Zhang Yan⁴,Huang Lihua⁴,Zhu Yun⁴,Lu Lifeng⁴,Zhong Wei⁴,Zeng Jixiao⁴,Xia Huimin¹⁴^ORCID

Affiliation:

1. The First Affiliated Hospital of Jinan University Guangzhou China

2. Guangzhou Medical University Guangzhou Guangdong China

3. Department of Neonatology Guangzhou Baiyunshan Hospital Guangzhou Guangdong China

4. Department of Pediatric Surgery Guangzhou Institute of Pediatrics Guangzhou Women and Children’s Medical Center Guangzhou Medical University Guangzhou Guangdong China

Funder

Natural Science Foundation of Guangdong Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.16905

Reference37 articles.

1. The developmental etiology and pathogenesis of Hirschsprung disease

2. Molecular genetics of Hirschsprung’s disease

3. A meta-analysis of clinical outcome in patients with total intestinal aganglionosis

4. An epidemiological study of Hirschsprung's disease and additional anomalies

5. Total colonic aganglionosis in Hirschsprung disease

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